United States · FDA National Drug Code directory

FASENRA

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0310-1745_b78fbf2b-888c-41e2-bdab-cb5cd1ebb8fe
Product NDC
0310-1745
Form
INJECTION, SOLUTION
Composition / generic term
Benralizumab
Labeler
AstraZeneca Pharmaceuticals LP
Marketing category
BLA
Marketing start / end (source format)
20240405
Source listing expiry
20271231

Source-listed ingredients

  • BENRALIZUMAB — 10 mg/.5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 CARTRIDGE in 1 CARTON (0310-1745-01) / .5 mL in 1 CARTRIDGE · 0310-1745-01
  • 1 CARTRIDGE in 1 CARTON (0310-1745-95) / .5 mL in 1 CARTRIDGE · 0310-1745-95

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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FASENRA — United States | Molindra Medicines